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Fructosuria

A benign hereditary defect of FRUCTOSE metabolism that results in a sharp increase in fructose excretion in the urine following ingestion of dietary fructose, SUCROSE, or SORBITOL. It is caused by mutations in the ketohexokinase (KHK) gene. OMIM: 229800
Also Known As:
Essential benign fructosuria; Hepatic fructokinase deficiency; Ketohexokinase deficiency
Networked: 25 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Experts

1. González-Devia, Deyanira: 1 article (01/2019)
2. Lemus, Hernan Nicolas: 1 article (01/2019)
3. Mendivil, Carlos O: 1 article (01/2019)
4. Morales-Alvarez, Martha Catalina: 1 article (01/2019)
5. Ricardo-Silgado, Maria Laura: 1 article (01/2019)
6. Akiyama, Taro E: 1 article (01/2018)
7. Askew, Roger: 1 article (01/2018)
8. Cao, Jin: 1 article (01/2018)
9. Herath, Kithsiri: 1 article (01/2018)
10. Li, Cai: 1 article (01/2018)

Related Diseases

1. Fructose Intolerance (Intolerance, Fructose)
2. Fructose-1,6-Diphosphatase Deficiency (Fructose 1,6 Diphosphatase Deficiency)
3. Hypoglycemia (Reactive Hypoglycemia)
4. Pentosuria
5. Metabolic Syndrome (Dysmetabolic Syndrome X)

Related Drugs and Biologics

1. Fructose
2. 3' Untranslated Regions (3' UTR)
3. Diphosphates (Pyrophosphates)
4. Proteins (Proteins, Gene)
5. Mercury
6. Ketone Bodies
7. Fructose-Bisphosphate Aldolase (Aldolase)
8. Enzymes
9. Cortisone
10. Carbohydrates